EndogenousTestosterone Response to a Testosterone Boosting Supplement

Testosterone Clinical Trial

Official title: EndogenousTestosterone Response to a Testosterone Boosting Supplement

Status Not yet recruiting

Clinical Trial Summary

The purpose of this study is to determine whether a proprietary 'testosterone-boosting' supplement, when used as recommended by the manufacturer, results in an increase in testosterone levels as measured by a salivary free testosterone assay.

Clinical Trial Description

The experimental intervention in this study is the daily administration of a testosterone boosting supplement or sham supplement for 4 weeks. The supplement will be administered daily in capsule form. The control group will be given a sham capsule containing the carrier components of the supplement. Participants will be asked not to modify their current lifestyle. Salivary testosterone levels will be assessed prior to the intervention to collect a baseline measurement for each subject, and following the intervention to evaluate any changes in hormone levels. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)

Related Conditions & MeSH terms

• Testosterone

• NCT number: NCT02600650
• Study type: Interventional
• Source: Canadian Memorial Chiropractic College
• Contact: mark fillery, B.A.
• Phone: +1 416 482-2340
• Email: mfillery@cmcc.ca
• Status: Not yet recruiting
• Phase: N/A
• Start date: November 2015
• Completion date: June 2016